Cited by 26Advanced Drug Delivery SystemsNanoparticle-Based Drug DeliveryRetinal Diseases and Treatments

The DOI matches its Crossref record; 38 of the 38 references it cites were found in a registry or an index.

Safety assessment of polymeric micelles as an ophthalmic drug delivery system for intravitreal administration of dasatinib

Li, Qingqing, Qian, Xiaobing, Li, Ho Yin, Lai, Ka Lun, Gao, Qianying, Lee, Wai Yip Thomas·2021·International Journal of Pharmaceutics

Abstract

Background and aims Ocular safety/biocompatibility is an essential element of ophthalmic drug delivery. We previously applied poly(ethylene glycol)-block-poly(ɛ-caprolactone) (PEG-b-PCL) micelles to deliver dasatinib for the management of proliferative vitreoretinopathy (PVR) in vitro. Herein, we seek to ascertain the ocular safety/compatibility of blank and dasatinib loaded PEG-b-PCL micelles, which will set the stage for the future in vivo efficacy evaluations and/or clinical translation for PVR or other eye diseases.Methods To access the safety of blank and dasatinib loaded micelles, in vitro cell based assays (LDH cell membrane damage test, SRB cytotoxicity, TEER and permeability of RPE tight junctions), in vivo slit lamp biomicroscopy and optical coherence tomography, Ex vivo histology (H&E staining, GFAP immunofluorescence staining and TUNEL assay) were undertaken.Results Both blank and dasatinib loaded micelles showed remarkable safety profiles at cellular levels. They also caused negligible ocular toxicity/abnormalities up to 28 days post-intravitreal injection in mice. The micelles did not insult the cornea, as demonstrated by slit-lamp biomicroscopy. Ex vivo histology and in vivo optical coherence tomography revealed a normal retinal structure with minimal apoptosis and stresses.Conclusion Taken together, both blank and dasatinib loaded micelles appear to be safe and their applications in drug delivery for eye diseases should be explored.

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Crossref · 10.1016/j.ijpharm.2021.120226

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  1. Groot, R.D., Rabone, K.L. Mesoscopic simulation of cell membrane damage, morphology change and rupture by nonionic surfactants. (0006-3495 (Print)). doi:D - NLM: PMC1301549 EDAT- 2001/07/21 10:00 MHDA- 2001/10/19 10:01 CRDT- 2001/07/21 10:00 AID - S0006-3495(01)75737-2 [pii] AID - 10.1016/S0006-3495(01)75737-2 [doi] PST – ppublish. · DOI

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Metadata

Authors
Li, Q., Qian, X., Li, H. Y., Lai, K. L., Gao, Q., & Lee, W. Y. T.
Affiliations
  • Chinese University of Hong Kong (HK)
  • Sun Yat-sen University (CN)
Venue
International Journal of Pharmaceutics
Publisher
Elsevier BV
Published
2021-03
Volume
596
Pages
120226
ISSN
0378-5173 (ISSN-L)
OpenAlex
W3125779010
Cited by
26
References
38
Citations by year
2026: 3 · 2025: 7 · 2024: 4 · 2023: 6 · 2022: 6
FWCI
1.61
Type
journal article
Language
en
Open access
closed
Locations
  • International Journal of Pharmaceutics (publishedVersion)
  • PubMed (publishedVersion)
Funders
Chinese University of Hong Kong
Topics
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
  • Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
  • Health Sciences › Medicine › Ophthalmology › Retinal Diseases and Treatments
Keywords
polymeric micelles, PEG-b-PCL, dasatinib, intravitreal drug delivery, eye safety, biocompatibility, proliferative vitreoretinopathy, retinal pigment epithelium, tight junction permeability, ocular toxicity, apoptosis, eye diseases
MeSH terms
Dasatinib, Animals, Cell Survival, Drug Carriers, Micelles, Polyesters, Polyethylene Glycols, Polymers, Drug Delivery Systems, Mice

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